The Chromosome 7 Annotation Project
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Chromosome 7 Clinical table -- PLUS 7 AND MARKER 7 (Non Malignant)

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# Unique IDKaryotypePhenotypeCytogenetic Break FromCytogenetic Break ToMolecular Breakpoint #1Molecular Breakpoint #2Pubmed IDPatient ID          Comments          
1 16317300_1 47, XY, upd(7) mat, +mar [9]. ish mar(7)(p11.2q11.21)(AC023141/ Q9BWX6/ D7S619+, D7Z1+, AC017075+)/ 46, XY, upd(7)mat [16] pre- & post-natal growth retardation, triangular face, relative macrocephaly, mild psychomotor retardation, ear anomalies, squeaky voice - some features of Silver-Russell syndrome p11.2 q11.21 D7S674/ AC023141 D7S2429/ D7S663 16317300   maker 7 - paternal origin Edit
2 13680362_12 47, XX, +mar [10] de novo/ 46, XX [12] [amniocytes]
7p+; cep 7+ min(7)(:p11.2-> q11.1:) [subcenM-FISH]
phenotypically normal p11.2 q11.2     16434320     Edit
3 18852357_1 mos 47,XY,+r(7)(p11.2q11.21)[22]/4 6,XY,upd(7) mat myoclonus-dystonia syndrome, Silver-Russell syndrome, intrauterine growth retardation, growth retardation, premature puberty, dystonia, myoclonus, small triangular-shaped face, prominent forehead, hypertelorism, smallmouth with thin lips,micrognathia with pointed chin, low posterior-rotated andoverfolded ears p11.2 q11.21 RP5-1091E12 RP11-340I6 18852357     Edit
4 Shimizu_A413 47, XX, +7p dysmorphic face, congenital heart defects, arched eyebrows, hypertelorism, low-set and malformed ears, broad nose, micrognathia, highly arched palate, short and webbed neck, hip joint dislocation and overlapped fingers pter p10       Shimizu et al., abstract, A413 Edit
5 6733951 47, XX, +7 [12%]/ 46, XX [88%] Potter syndrome, pulmonary hypoplasia, renal agenesis, died 14 hrs after birth pter qter     6733951, 10594874, 12124684, 16092121     Edit
6 8411076 47, XY, +7 [9] [amniotic fluid, 1st culture]
46, XY [30] [amniotic fluid, 2nd culture]
46, XY [60] [blood, aged 7]
47, XY, +7 [23]/ 46, XY [13] [skin, aged 8]
hypomelanosis of Ito, mild developmental delay, facial asymmetry, cleft uvula, enamel dysplasia pter qter     8411076, 9110367, 10594874, 16092121, 12124684, 16302164 VII-4 [9110367]   Edit
7 10594874_1 46, XY [293]/ 47, XY, +7 [56]/ 46, XY, r(7) [60]/ 47, XY, +7, r(7)[2] intrauterine growth retardation, short stature, moderate mental retardation, multiple minor anomalies, pigmentation anomalies pter qter     10594874     Edit
8 7390476 47, XX, +7 de novo Potter syndrome, hypertelorism, depressed nasal bridge, low-set ears, micrognathia, short neck, narrow pelvis, bilateral clubfoot, hypotonicity, anal imperforation, abnormal external genitals, no opening to vagina, vertebral abnormalities, polycystic and hydronephrotic kidney, hypoplastic lungs pter qter     7390476, 6733951, 10594874, 12407716   twin brother had normal karyotype Edit
9 10594873 47, XY, +7 [28]/46, XY [7] [skin] linear and whorled nevoid hypermelanosis, hypomelanosis of Ito, Dandy-Walker variant, developmental delay, hypotonia, pyschomotor delay, heart defect (PDA & VSD), asymmetric ptosis, short downslanting palpebral fissures, sparse eyelashes pter qter     10594873, 10594874     Edit
10 Unpublished_54 46, XY, mar(7) cognitive delay, emotional difficulties, mild dysmorphic features, multiple pigmented nevi pter qter     54 data unpublished Edit
11 7341641 47, XX, +7/ 46, XX [skin-right forearm]
46, XX [blood, skin-left forearm]
plagiocephaly, abnormalities of left ear, facial asymmetry, abnormalities of head hair pattern, cleft lip and palate, bifid tongue, left torticollis, hemivertebrae, left radial hypoplasia and absent thumb, left inguinal hernia, patient ductus arteriosus, narrowing of the thoracic aorta, and hypoplastic right pulmonary artery pter qter     7341641, 10594874, 12124684, 16092121     Edit
12 12128070 47, X?, +7 primary osteorarthritis of the knee/hip pter qter     12128070   synovial cells Edit
13 424118 47, XX, +7 de novo phenotype not given pter qter     424118   trisomy due to nondisjunction of the second maternal meiotic division Edit
14 3812554 47, XY, +7 [42]/ 46, XY, +7 with random loss [3]/ 46, XY [11] [umbilical cord cells]
46, XY [21] [skin fibroblasts]
low-set ears, flattened face, renal dysplasia, pulmonary hypoplasia pter qter     3812554, 12124684, 12407716, 16092121     Edit
15 1142382 47, XX +7 [14%]/ 46, XX [86%] histeria pter qter     1142382, 10594874, 16092121 mother daughter also had trisomy 7 mosaicism [9%] Edit
16 ECACC_92112305 48, XX, +7, +8 phenotype abnormal pter qter     92112305 (cell line: DD1078) 3rd consecutive miscarriage, IVF pregnancy; www.ecacc.or.uk Edit
17 ECACC_93080511 46, XX, mar(7) developmental delay, autism pter qter     93080511 (cell line: CC0096) www.ecacc.or.uk Edit
18 ECACC_95030626 46, XY/ 47, XY, +7 phenotypically normal pter qter     95030626 (cell line: DD2221) fetus; chorionic villi sample for maternal age 43; 50% cells in this culture had +7; www.ecacc.or.uk Edit
19 NIGMS_GM03913 46, XY [46%]/ 47, XY, +7 [54%] Roberts Syndrome (RBS) pter qter     GM03913 fibroblast, finite (primary) cell line from CCR: NIGMS Human Genetic Cell Repository Edit
20 NIGMS_GM09812 46, XX [92%]/ 47, XX, +7 [4%]/ 47, XX, +18 [4%] qter pter       GM09812 lymphoblast: 46,XX/47,XX,+ 12; fibroblast, finite (primary) cell line from CCR: NIGMS Human Genetic Cell Repository Edit
21 NIGMS_GM14084 45, XX, -3 [2]/ 45, XX, -17 [2]/ 45, XX, -22 [2]/ 46, XX [88]/ 47, XX, +7 [4]/ 47, XX, +8 [2]/ 47, XX, +14 [2] severe microcephaly, developmental delay pter qter     GM14084 fibroblast, finite (primary) cell line from CCR: NIGMS Human Genetic Cell Repository Edit
22 1756501 48, XY, +7, +i(12)(p10) [24] 46,XY female, mixed gonadal dysgenesis -teratoma (mature and immature) and yolk sac elements pter qter     1756501   Mitelman Database, Reference No. 4090 Edit
23 8923948 47, X?, +7/ 46, X? 2 of 14 were small for gestational age; the rest were normal pter qter     8923948, 9106539 14 cases 14 pregnancies diagnosed by CVS; follow-up amniocentesis showed normal karyotype Edit
24 15337469_1 47, XX, +mar. ish r(7)(p?q?)(D7Z1+, ELN+) [38]/ r(7)(D7Z1++, ELN++) [2] de novo / 46, XX [12] mild motor developmental delay, broad forehead, asymmetrical facial appearance, plagiocephaly, short nose with anteverted nostrils, long and slender extremities, moderate deafness pter q21.2   ELN/ D7S522 15337469 case 1 in 4% of the cells analyzed, maker r(7) was duplicated and dicentric (D7Z1, ELN) Edit
25 15337469_2 47, XY, +mar. ish r(p?q?)(D7Z1+, ELN+) [48]/ r(7)(D7Z1++, ELN++) [2] de novo / 46, XY [50] borderline performance, obesity, hyperactivity with fits of anger, speech difficulties, hypertelorism, down-slanting palpebral fissures, IQ of 80 pter q11.2     15337469 case 2 in 2% of the cells analyzed, maker r(7) was duplicated and dicentric (D7Z1, ELN) Edit
26 von Beust_ESHG2004 47, XX, +mar [26]/ 46, XX [14] [marker was derived from chr. 7] congenital heart defect, dysmorphic features pter qter       von Beust et al., ESHG 2004, P0172 Edit
27 12605443 47, XX, +7 [13]/ 46, XX [19] [amniocytes]
47, XX, +7 [50] [cord blood]
47, XX, +7 [19] [postpartum chorionic villus]
47, XX, upd(7)mat, +7 [9]/ 46, XX, upd(7)mat [20] [skin]
upd(7)mat [confirmed by microsatellite markers, peripheral blood]
posterior-rotated low-set ears, prominent forehead, small chin, triangular face, obstructed left nares, prominent nasal bridge, reversed epicanthal folds, thin lips, small mouth, micrognathia, bilateral clinodactyly of V finger, bridged Simian crease on left hand pter qter     12605443, 16007591, 16302164   trisomy 7- two maternal and one paternal chromosomes & maternal uniparental heterodisomy Edit
28 16092121 47, XX, +7 [12]/ 45, X [2] hypopigmentation and hyperpigmentation following the Blaschko lines, growth retardation, buphthalmos of the left eye, mild mental retardation pter qter     16092121     Edit
29 953215 47, XY, +C [possibly, +7] flattened nasal bridge, posteriorly rotated low-set ears, prominent occiput, short neck, tapered fingers, clinodactyly of 5th dingers, bilateral diffuse renal dysplasia, pulmonary hypoplasia, died 17 hours after birth pter qter     953215, 6733951, 10594874   Trisomy 11 (+C) was suggested in the first paper [953215] Edit
30 5420797 47, X?, +C de novo [possibly, +7] flattened nasal bridge, epicanthic folds, micrognathia, low-set ears, midline cleft palate, hyperextensible joints, bilateral hip dislocation, bilateral polycystic disease of the kidneys (type II), polycystic ovaries, died one hour after birth pter qter     5420797, 6733951, 10594874     Edit
31 15953408 46-47, X, +7, -X [cp18]
XXX (74%), X (13%), XXXX (3%), XX (10%) [amniotic fluid cell, by FISH]
XXX (75%), X (11%), XXXX (6%), XX (8%) [cord blood, by FISH]
IUGR, severe oligohydramnios, dysmorphic features, abnormal external genitalia, Potter syndrome, mesomelic dysmorphism [indicated by X-ray] pter qter     15953408 aborted fetus at 32nd week   Edit
32 8411070 46, XX [lymphocytes & dark skin fibroblasts]
47, XY, +7/ 46, XX [light skin keratinocytes]
developmental delay, epilepsy severely visually impaired, minimal white streaks on the right flank, hip and leg pter qter     8411070, 16092121     Edit
33 12124684 47, XY, +7 [7]/ 46, XY [2] [amniotic fluid, 16 wks' gestation]
46, XY [blood, 20 wks' gestation]
46, XY [blood, 3yr 6m]
47, XY, +7 [36]/ 46, XY [64] [pigmented skin, 3yr 6m]
47, XY, +7 [24]/ 46, XY [76] [hypopigmented skin, 3 yr 6m]
facial asymmetry, congenital ptosis of left eye, facial paresis on left side, short left palpebral fissure, hypotonic, hypopigmentation on trunk and limbs following Blaschko's lines, enamel dysplasia, low-set & posteriorly rotated ears, sparse hair, undescended testes pter qter     12124684, 16302164 proband   Edit
34 11102936 47, XY, +7 [43%]/ 46, XY [57%] [skin]
47, XY, +7 [3%]/ 46, XY [97%] [skin, second culture]
46, XY [100%] [blood]
developmental delay, asymmetrical growth, mixed receptive-expressive language disorder, Blaschkolinear skin pigmentary changes (hypo-/hyperpigmentation), aggressive behaviour pter qter     11102936 JB   Edit
35 9110367_VII-1 47, XY, +7 [48%]/ 46, XY [amniocytes]
46, XY [60] [blood]
46, XY [10] [skin]
phenotypically normal at 4.5 years of age pter qter     9110367, 16302164 VII-1, AF9640   Edit
36 9110367_VII-2 47, XY, +7 [36.6%]/ 46, XY [amniocytes]
46, XY [203] [cord blood]
46, XY [100] [blood]
47, XY, +7 [18]/ 46, XY [20] [foreskin]
phenotypically normal at 4 years of age pter qter     9110367, 16302164 VII-2, A1336-91   Edit
37 9110367_VII-3 47, XX, +7 [5%]/ 46, XX [amniocytes]
46, XX [blood & placenta]
phenotypically normal at birth pter qter     9110367, 16302164 VII-3   Edit
38 9110367_VII-5 47, XX, +7 [31.3%]/ 46, XX [amniocytes]
46, XY [30] [amniotic fluid]
46, XX [CVS]
phenotypically normal at birth pter qter     9110367, 16302164 VII-5, case KW   Edit
39 9110367_VII-6 47, XX, +7 [26.7%]/ 46, XX [amniocytes] phenotypically normal at birth pter qter     9110367, 16302164 VII-6, case AA   Edit
40 9110367_VII-7 47, XY, +7 [15%]/ 46, XY [amniocytes]
46, XY [30] [cord blood]
phenotypically normal at 25 months of age pter qter     9110367, 16302164 VII-7, 41023   Edit
41 9110367_VII-8 47, XY, +7 [40%]/ 46, XY [amniocytes] phenotypically normal at 4 months of age pter qter     9110367, 16302164 VII-8, A94-28241   Edit
42 9855612 48, XY, +4, +7 [20] phenotype not given - mother had incomplete abortion at the gestational age was 8~9 weeks [detected ultrasound] pter qter     9855612 abortus mother was 42 years old Edit
43 10213044 47, XY or XX, +7 phenotype not given; mother had spontaneous abortion pter qter     10213044 12 cases (T7-1 to -12) maternal origin - 9 cases, paternal origin - 1 case, origin not determined - 2 cases; meiotic trisomy - 10 cases, mitotic trisomy(?) - 2 cases Edit
44 9832040 47, XY or XX, +7 phenotype not given; mother had spontaneous abortion pter qter     9832040 15 cases maternal origin - 12 cases, paternal origin - 2 cases, origin not determined - 1 case; maternal meiotic trisomy - 6 cases, mitotic trisomy(?) - 8 cases, unknown - 1 case Edit
45 9556035 47, XX, +7 [11]/ 46, XX [14] [CVS]
46, XX [21] [long-term culture]
46, XX [30] [amniotic fluid]
phenotype not given pter qter     9556035 case 2   Edit
46 3399481 47, XX, +7 [CVS]
46, XX [amniotic fluid cels]
46, XX [12] [placenta, central]
47, XX, t(2;21)(p13;q22), +20 [12]/ 46, XX [30] [placenta, peripheral]
46, XX [100] [cord blood]
phenotypically normal at birth pter qter     3399481     Edit
47 9483638 47, XY or XX, +7/ 46, XY or XX phenotypically normal on birth pter qter     9483638 cases 5, 6, 8 -10 % of trisomic cells ranged from 9 to 40% Edit
48 9439664_1 48, XXX, +7 phenotype not given; mother had spontaneous abortion pter qter     9439664 case 1   Edit
49 9439664_21 48, XX, +7, +12 [22]/ 46, XX [2] phenotype not given; mother had spontaneous abortion pter qter     9439664 case 21   Edit
50 9316135 48, XX, +7, +20 [4]/ 46, XX [4] [amniotic fluid, 16 wks]
48, XX, +7, +20 [15] [amniotic fluid, 20 wks]
46, XX [20] [CVS, 20 wks]
46, XX [30] [blood & fibroblast at birth]
phenotypically normal pter qter     9316135     Edit
51 8655147_1 47, XX, +7 [27%]/ 46, XX [CVS]
47, XX, +7 [0-37%]/ 46, XX [term placenta]
phenotypically normal, normal birth weight pter qter     8655147 case 1   Edit
52 8655147_6 47, XX, +7 [17%]/ 46, XX [CVS]
47, XX, +7 [0-27%]/ 46, XX [term placenta]
phenotypically normal, normal birth weight pter qter     8655147 case 6   Edit
53 11464246_MZ-570 47, XX, +7. rev ish enh(7) phenotype not given; mother had spontaneous abortion pter qter     11464246 MZ-570   Edit
54 11464246_MR-120 47, XX, +7. rev ish enh(7) phenotype not given; mother had spontaneous abortion pter qter     11464246 MR-120 maternal origin Edit
55 11464246_MR-137 47, XY, +7. rev ish enh(7) phenotype not given; mother had spontaneous abortion pter qter     11464246 MR-137 paternal origin Edit
56 16302164 47, XX, +7 [3]/ 46, XX [15] [amniocytes, 17 wks]
47, XX, +7 [3]/ 46, XX [22] [amniocytes, at 18 wks]
46, XX [40] [CVS, 18 wks]
46, XX [40] [cord blood, placenta, liver, lungs, skin]
phenotypically normal; pregnancy was terminated pter qter     16302164     Edit
57 7316468 48, XY, +7, +10 phenotype not given; mother had spontaneous abortion pter qter     7316468   advanced maternal age - 37 years old Edit
58 1804088 47, XY, +7 [3]/ 46, XY [5] [CVS]
47, XY, +7/ 46, XY & 47, XY, +7 [placenta]
46, XY [blood, at birth]
phenotypically normal pter qter     1804088     Edit
59 8878279_33 47, XY, +7 [3]/ 46, XY [8] [cytotrophoblasts]
46, XY [fetal cells after abortion]
phenotype not given; pregnancy was terminated because of X-linked disease pter qter     8878279 case 33   Edit
60 8878279_101 47, XY, +7 [2]/ 46, XY [14] [cytotrophoblasts]
46, XY [amniocytes]
phenotype not given; pregnancy was continued pter qter     8878279 case 101   Edit
61 8878279_14 47, XY, +7 [3]/ 46, XY [12] [cytotrophoblasts]
46, XY [amniocytes]
phenotype not given; pregnancy was continued pter qter     2803989, 8878279 case 14   Edit
62 8878279_102 47, XY, +7 [13]/ 46, XY [4] [cytotrophoblasts]
46, XY [amniocytes]
phenotype not given; pregnancy was continued pter qter     8878279 case 102   Edit
63 8878279_73 47, XX, +7 [4]/ 46, XY [13] [cytotrophoblasts]
46, XX [amniocytes]
phenotype not given; pregnancy was continued pter qter     8878279 case 73   Edit
64 8878279_55 49, XY, +3, +4, +7 [2]/ 48, XY, +3, +7 [1]/ 46, XY [14] [cytotrophoblasts]
46, XY [amniocytes]
phenotype not given; pregnancy was continued pter qter     8878279 case 55   Edit
65 8878279_78 48, XY, +4, +7 [3]/ 47, XY, +4 [3]/ 46, XY [8] [cytotrophoblasts]
46, XY [amniocytes]
phenotype not given; pregnancy was continued pter qter     8878279 case 78   Edit
66 8878279_105 55, XYY, +2, +3, +5, +7, +8, +11, +15, +20 [6]/ 46, XY [16] [cytotrophoblasts]
46, XY [amniocytes]
phenotype not given; pregnancy was continued pter qter     8878279 case 105   Edit
67 8878279_13 50, XY, +2, +3, +7, +15 [5]/ 46, XY [28] [cytotrophoblasts]
46, XY [amniocytes]
phenotype not given; pregnancy was continued pter qter     2803989, 8878279 case 13   Edit
68 2235900_1 46, XY [CVS, direct]
47, XY, +7 [34%]/ 46, XY [66%] [CVS, culture]
47, XY, +7 [placenta, culture]
fatal demise detected by ultrasound at 15.5 weeks of gestation pter qter     2235900 case 1 (2061-88)   Edit
69 2235900_2 46, XY [CVS, direct]
47, XY, +7 [53%]/ 46, XY [47%] [CVS, culture]
47, XY, +7 [8%]/ 46, XY [92%] [placenta, culture]
46, XY [cord blood & skin]
phenotypically normal at birth pter qter     2235900 case 2 (2092-89)   Edit
70 3799715 47, XX, +7 [34]/ 46, XX [28] [CVS]
46, XX [100] [skin & umbilical cord]
phenotype not given; pregnancy was terminated at 10 weeks of gestation pter qter     3799715     Edit
71 3228150 47, XY +7 [12]/ 46, XY [30] [CVS, culture 1]
47, XY +7 [11]/ 46, XY [36] [CVS, culture 2]
47, XY +7 [6]/ 46, XY [55] [CVS, culture 3]
47, XY +7 [1]/ 46, XY [30] [CVS, culture 4]
46, XY [100%] [fatal blood & amniotic fluid culture at 19 wks]
phenotype not given pter qter     3228150     Edit
72 6475960 52, XX, +2, +7, +8, +12, +13, +20/ 46, XX [clitoral mass]
46, XX [blood & ovary]
ambiguous genitalia, clitoral mass; otherwise phenotypically normal pter qter     647596     Edit
73 655633 47, XY, +7 phenotype not given; mother had repeated spontaneous abortions pter qter     655633   1 of 234 spontaneous abortion cases had trisomy 7 Edit
74 6331788 47, XY, +7 [100%] several malformations including severe anomalies of the splenomesenteric vascular system, persistence of Mullerian ducts, major anomalies of the anterior chamber of eye, facial dysmorphism; died at 3 months after birth pter qter     6331788 patient 240578   Edit
75 8125474_3 47, XX, +7 [5]/ 46, XX [45] [amnion] phenotype not given pter qter     8125474 3   Edit
76 7450760 48, XX, +7, +22 phenotype not given; mother had spontaneous abortion pter qter     7450760 spontaneous abortus one of 447 spontaneous cases karyotyped Edit
77 3580545 48, XX, +2, +7 phenotype not given; mother had spontaneous abortion pter qter     3580545 spontaneous abortus one of 460 early spontaneous cases karyotyped Edit
78 4063875 48, XXX, +7 phenotype not given; mother had spontaneous abortion pter qter     4063875, 9439664 spontaneous abortus one of 215 spontaneous abortion cases karyotyped Edit
79 9483638_7 48, XY, +7, +9 [2]/ 46, XY [17] [CVS] phenotypically normal on birth pter qter     9483638 case 7   Edit
80 18352813 47~48,XX,+der(7)t(7;7)(p22;?),+ der(7)(7?::7p22→7q11:: 7?)[cp7] papillary glioneuronal tumor pter qter     18352813     Edit
81 18397339_SE11 47,XY [-6(q13-q15),+ 7 detected by microarray] subependymoma tumor in fourth ventricle pter qter     18397339 SE11   Edit
82 18587327_2 4?, X?,+7 adenoid cystic carcinoma pter qter     18587327 case 2 observed in 4 of 12 (33%) cases Edit
83 18587327_6 4?, X?,+7 adenoid cystic carcinoma pter qter     18587327 case 6 observed in 4 of 12 (33%) cases Edit
84 18587327_10 4?, X?,+7 adenoid cystic carcinoma pter qter     18587327 case 10 observed in 4 of 12 (33%) cases Edit
85 18587327_11 4?, X?,+7 adenoid cystic carcinoma pter qter     18587327 case 11 observed in 4 of 12 (33%) cases Edit
86 18587327_13 4?, X?,+7 mucoepidermoid carcinoma pter qter     18587327 case 13 observed in 2 of 12 (17%) cases Edit
87 18587327_23 4?, X?,+7 mucoepidermoid carcinoma pter qter     18587327 case 23 observed in 2 of 12 (17%) cases Edit
88 18452823_1 46, XY.nuc ish +7 [68%], +17 [76%] type 1 papillary renal carcinoma pter qter     18452823 Patient 1 sibling of 18452823_2, mother also affected by PRC Edit
89 18452823_2 46, XY.nuc ish +7 [60%], +17 [66%], -Y [80%] type 1 papillary renal carcinoma pter qter     18452823 Patient 2 sibling of 18452823_1, mother also affected by PRC Edit
90 18795325 47,XY,+7 end-stage kidney disease pter qter     18795325   observed in 6 of 11 cases Edit
91 18592004_132 4?,XY,+7 [detected by microarray] renal cell carcinoma pter qter     18592004 Case 132 observed in 32% of cases, discussion of FZD9, MET, EPHA1 as candidate genes Edit
92 18592004_135 4?,XY,+7 [detected by microarray] renal cell carcinoma pter qter     18592004 Case 135 observed in 32% of cases, discussion of FZD9, MET, EPHA1 as candidate genes Edit
93 18592004_139 4?,XY,+7 [detected by microarray] renal cell carcinoma pter qter     18592004 Case 139 observed in 32% of cases, discussion of FZD9, MET, EPHA1 as candidate genes Edit
94 18592004_154 4?,XY,+7 [detected by microarray] renal cell carcinoma pter qter     18592004 Case 154 observed in 32% of cases, discussion of FZD9, MET, EPHA1 as candidate genes Edit
95 18592004_163 4?,XY,+7 [detected by microarray] renal cell carcinoma pter qter     18592004 Case 163 observed in 32% of cases, discussion of FZD9, MET, EPHA1 as candidate genes Edit
96 18779729_1 4?,XX,del(3)(p25p25)+7[65%],+ 17[47%] renal cell carcinoma pter qter     18779729 Case 1   Edit
97 18779729_3 4?,XX,+7[64%],+ 17[36%] papillary renal cell carcinoma pter qter     18779729 Case 3   Edit
98 18779729_4 4?,XY,-Y[98%],+7[60%],+ 17[28%] papillary renal cell carcinoma pter qter     18779729 Case 4   Edit
99 18779729_5 4?,XY,-Y[100%],+7[44%],+ 17[12%] papillary renal cell carcinoma pter qter     18779729 Case 5   Edit
100 18779729_6 4?,XX,+7[46%],+ 17[40%] papillary renal cell carcinoma pter qter     18779729 Case 6   Edit
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